- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07578571
A Phase 1 Study of IM-1617 in Participants With Advanced Cancer
A Phase 1 Study of IM-1617 in Participants With Advanced Malignancies
This study will test the safety and effectiveness of a drug called IM-1617 in participants with solid tumors. Participants will have solid tumor cancer that has spread through the body (metastatic) or cannot be removed with surgery (unresectable).
This study will have two parts. Part A will test increasing doses of IM-1617 to find out the safe dose and schedule of IM-1617 for participants. Part B will use the dose and schedule found in Part A to further study the safety of IM-1617 and if it works to treat solid tumor cancers.
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
This is a Phase 1 open-label, multicenter, dose escalation and expansion study designed to determine the safety, tolerability, PK, and preliminary antitumor activity of IM-1617 administered to participants with unresectable locally advanced or metastatic solid tumors. The study consists of 2 parts:
Part A: A dose-escalation phase to evaluate the safety and tolerability of IM-1617 to determine the recommended dose for expansion (RDE), evaluate maximum tolerated dose, and maximum achievable dose of IM-1617 in up to approximately 75 participants.
Part B: An expansion phase to further evaluate the safety and preliminary antitumor activity of IM-1617 monotherapy at the RDE and one or more other dose regimens in up to 4 indication-specific cohorts. Up to approximately 100 participants will be enrolled in Part B.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Immunome Medical Monitor
- Telefonnummer: 425.939.7410
- E-mail: IM-1617-101@immunome.com
Studiesteder
-
-
Texas
-
Irving, Texas, Forenede Stater, 75039
- Rekruttering
- NEXT Dallas
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
Part A: Histological diagnosis of one of the following unresectable locally advanced or metastatic solid tumors:
- CRC, all subtypes
NSCLC:
- Non-squamous cell carcinoma subtypes, such as adenocarcinoma
- Squamous cell carcinoma subtype
Breast cancer (subtypes based on estrogen/progesterone receptor and HER2 testing according to American Society of Clinical Oncology - College of American Pathologists guidelines):
- Triple-negative breast cancer
- HR+, HER2- subtype
Esophageal, esophagogastric junction, and gastric cancer:
- Adenocarcinoma subtype
- Other histologies, if approved by the Medical Monitor, which may include: head and neck squamous cell carcinoma; cervical cancer; bladder cancer; squamous cell carcinoma subtype of esophageal, esophagogastric junction, and gastric cancer; HER2+ breast cancer
Part B Cohorts - Histological diagnosis of one of the following unresectable locally advanced or metastatic solid tumors:
- Cohort B1: CRC, all subtypes
Cohort B2: NSCLC
- Non-squamous cell carcinoma subtypes, such as adenocarcinoma
- Squamous cell carcinoma subtype
- Cohorts B3 and B4: Cohort-specific disease indications may include those listed for Part A
Participants must have disease that is considered to be noncurative and meet the appropriate criteria below:
- Part A only: Participants have progressed on, were intolerant to, or have a contraindication to prior SOC treatments, with no satisfactory SOC treatment options available.
Part B only:
Cohort B1 (CRC):
- Participants must have previously progressed on, were intolerant to, or have a contraindication to fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, bevacizumab, and for those with RAS wild-type tumors, an anti-epidermal growth factor receptor (EGFR)-directed monoclonal antibody in advanced disease setting.
- Participants with actionable biomarkers must have been treated with at least one prior appropriate biomarker-directed therapy.
- If any of these therapies was given in the adjuvant setting, disease must have progressed within 6 months after completing therapy.
Cohort B2 (NSCLC):
- Participants must have previously progressed on, were intolerant to, or have a contraindication to platinum-based chemotherapy and a programmed cell death-1 (PD-1)/programmed death ligand 1 (PD-L1) monoclonal antibody (given concurrently or sequentially with chemotherapy) in advanced disease setting.
- Participants with actionable biomarkers must have been treated with at least one prior appropriate targeted therapy.
- If any of these therapies was given in the adjuvant setting, disease must have progressed within 6 months after completing therapy.
- Cohorts B3 and B4: Criteria will be specified based on the disease indications selected.
- Participants must have measurable disease as defined per RECIST v1.1
Exclusion Criteria:
- Previously treated with an antibody-drug conjugate (ADC) with a topoisomerase-1 (TOP1) inhibitor payload. Exception: Participants with NSCLC or breast cancer may have received up to one prior ADC with a TOP1 inhibitor payload
- History of anaphylactic reaction to TOP1 inhibitors (e.g., irinotecan) or TOP1 inhibiting ADCs
- Life expectancy < 12 weeks
- Prior solid organ transplant
- Symptomatic ascites or pleural effusion
- Known active central nervous system (CNS) metastases and/or carcinomatous meningitis
- Known history of another primary solid or hematologic malignancy (other than that under study), unless the participant has undergone potentially curative therapy with no evidence of recurrence for at least 2 years and approved by the Medical Monitor
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: IM-1617 Dose Escalation
IM-1617 given into the vein (IV; intravenously)
|
IM-1617 is an antibody-drug conjugate
|
|
Eksperimentel: IM-1617 Monotherapy Dose Expansion
IM-1617 given into the vein (IV; intravenously)
|
IM-1617 is an antibody-drug conjugate
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of adverse events (AEs) and serious adverse events (SAEs)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Type, frequency, seriousness, and severity of adverse events (AEs) graded using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 6.0
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of AEs of interest (AEIs)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Type, frequency, seriousness, and severity of adverse events (AEs) graded using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 6.0
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of AEs leading to discontinuation
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Type, frequency, seriousness, and severity of adverse events (AEs) graded using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 6.0
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of death
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Type, frequency, seriousness, and severity of adverse events (AEs) graded using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 6.0
|
Through 30 days after last dose of study treatment; approximately 12 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Characterize the PK of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by area under the concentration-time curve (AUC)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Pharmacokinetic (PK) parameter
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Characterize the PK of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by maximum observed concentration (Cmax)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
PK parameter
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Characterize the PK of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by time to maximum observed concentration (Tmax)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
PK parameter
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Characterize the PK of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by trough concentration (Ctrough)
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
PK parameter
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Characterize the immunogenicity of IM-1617
Tidsramme: Through 30 days after last dose of study treatment; approximately 12 months
|
Incidence of antidrug antibodies (ADA)
|
Through 30 days after last dose of study treatment; approximately 12 months
|
|
Evaluate the preliminary antitumor activity of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors
Tidsramme: From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
Objective Response Rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 as assessed by the Investigator
|
From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
|
Evaluate the preliminary antitumor activity of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors
Tidsramme: From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
Complete Response Rate (CRR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 as assessed by the Investigator
|
From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
|
Evaluate the preliminary antitumor activity of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors
Tidsramme: From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
Disease Control Rate (DCR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 as assessed by the Investigator
|
From start of study until disease progression by RECIST v1.1 or initiation of subsequent anticancer therapy; up to approximately 12 months
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer efter sted
- Tarmsygdomme
- Luftvejssygdomme
- Gastrointestinale neoplasmer
- Neoplasmer i fordøjelsessystemet
- Sygdomme i fordøjelsessystemet
- Gastrointestinale sygdomme
- Mavesygdomme
- Intestinale neoplasmer
- Endetarmssygdomme
- Lungesygdomme
- Neoplasmer i hoved og hals
- Neoplasmer i luftvejene
- Thoracale neoplasmer
- Tyktarmssygdomme
- Esophageale sygdomme
- Lungeneoplasmer
- Hudsygdomme
- Brystsygdomme
- Karcinom, bronkogent
- Bronkiale neoplasmer
- Hud- og bindevævssygdomme
- Neoplasmer
- Neoplasmer i maven
- Kolorektale neoplasmer
- Esophageale neoplasmer
- Brystneoplasmer
- Karcinom, ikke-småcellet lunge
Andre undersøgelses-id-numre
- IM-1617-101
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med IM-1617
-
Innovative Molecules GmbHAfsluttet
-
ONWARD Medical, Inc.RekrutteringRygmarvsskader | BlodtryksforstyrrelserForenede Stater
-
University of Illinois at ChicagoAfsluttetAkut myeloid leukæmi | Kronisk myeloid leukæmi | Akut leukæmi | Lymfoblastisk leukæmi | Non Hodgkins lymfomForenede Stater
-
Fundación Eduardo AnituaAfsluttet
-
University Hospital, Clermont-FerrandRekrutteringSlag | Multipel sclerose | Rygmarvsskade | HovedtraumeskadeFrankrig
-
University of PaviaRekruttering
-
STAT Therapeutics IncJohnson County ClinTrialsAfsluttetSund Frivillig - KompletForenede Stater
-
National Institute of Allergy and Infectious Diseases...Rekruttering
-
Ultragenyx Pharmaceutical IncAbeona Therapeutics, IncRekrutteringMucopolysaccharidosis III | Sanfilippo syndrom | MPS IIIA | Sanfilippo ASpanien, Forenede Stater, Australien
-
University Hospitals, LeicesterPublic Health England; Crucell Holland BV; National Institute of Biological...Afsluttet